EP0129338A2 - Electrolytic treatment method - Google Patents
Electrolytic treatment method Download PDFInfo
- Publication number
- EP0129338A2 EP0129338A2 EP84303393A EP84303393A EP0129338A2 EP 0129338 A2 EP0129338 A2 EP 0129338A2 EP 84303393 A EP84303393 A EP 84303393A EP 84303393 A EP84303393 A EP 84303393A EP 0129338 A2 EP0129338 A2 EP 0129338A2
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- EP
- European Patent Office
- Prior art keywords
- current
- graphite electrodes
- electrolytic
- electrode
- graphite
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N3/00—Preparing for use and conserving printing surfaces
- B41N3/03—Chemical or electrical pretreatment
- B41N3/034—Chemical or electrical pretreatment characterised by the electrochemical treatment of the aluminum support, e.g. anodisation, electro-graining; Sealing of the anodised layer; Treatment of the anodic layer with inorganic compounds; Colouring of the anodic layer
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S204/00—Chemistry: electrical and wave energy
- Y10S204/09—Wave forms
Definitions
- the present invention relates to a method of electrolytic treatment on the surface of metal web with which the stability of graphite electrodes used in the electrolytic treatment of a metal plate is remarkably improved.
- Examples of a method of applying an electrolytic treatment to the surface of a metal member made of aluminum, iron or the like are the plating method, the electrolytic roughening method, the electrolytic etching method, the anodic oxidation method, the electrolytic coloring method, and the electrolytic satin finishing method, all which have been extensively employed in the art.
- D.C. sources, power mains A.C. sources, superposed-waveform current sources, and thyristor-controlled special-waveform or square-wave A.C. sources have been employed with these methods in order to meet requirements of quality of the electrolytic treatment or to improve the reaction efficiency.
- GB 1,548,689 discloses a process in which an A.C. is applied in the electrolytic treatment of an aluminum plate with the voltage applied to the anode electrode being higher than that applied to the cathode electrode, whereby an aluminum
- FIG. 1 shows an example of a conventional continuous electrolytic treatment system for metal webs which utilizes graphite electrodes.
- a metal web 1 is introduced into an electrolytic cell 4. while being guided by a guide roll 2, and is conveyed horizontally through the cell while being supported by a roll 3. Finally, the web 1 is moved out of the cell passing around a guide roll 5.
- the electrolytic cell 4 is divided by an insulator 6 into two chambers in which graphite electrodes are arranged on both sides of the metal web 1.
- a supply of electrolytic solution 28 is stored in a tank 9.
- a pump 10 supplies the electrolytic solution 28 to electrolytic solution supplying pipes 11 and 12 which debouch into the electrolytic cell 4.
- the electrolytic solution thus supplied covers the graphite electrodes 7 and 8 and the metal web and then returns to the tank 9 through a discharging pipe 13.
- a power source 14 connected to the graphite electrodes 7 and 8 applies a voltage thereto.
- An electrolytic treatment can be continuously applied to the metal web 1 with this system.
- the power source 14 may produce (1) direct current, (2) symmetric alternate current waveform, (3) and (4) asymmetric alternate current waveform, and (5) and (6) asymmetric square-wave alternate current waveform as shown in Fig. 2.
- the average value of the forward current In is not equal to the average value of the reverse current I r .
- a graphite electrode is considerably stable when used as a cathode electrode.
- a graphite electrode is used as an anode electrode, it is consumed in the electrolytic solution, forming C0 2 by anode oxidation and, at the same time, it decays due to erosion of the graphite interlayers, which occurs at a rate depending on electrolytic conditions.
- the current distribution in the electrode changes so that the electrolytic treatment becomes nonuniform. Therefore, the occurrence of such a phenomenon should be avoided in a case where the electrolytic treatment must be done with high accuracy. Accordingly, it is necessary to replace the electrodes periodically. This requirement is a drawback for mass production, and is one of the factors which lowers productivity.
- the inventors have conducted intensive research regarding ways to prevent the consumption of graphite electrodes, and found conditions exist under which graphite electrodes employed in a system using asymmetric waveform A.C. can be stabilized.
- an asymmetric waveform current (In > I r ) as shown at (4) in Fig. 2 was used.
- the forward terminal was connected to the electrode 7 and the reverse terminal to the electrode 8.
- an electrolytic treatment was carried out by using a 1% HC1 electrolytic bath with a current density of 50 A/dm 2 and a frequency of 60 Hz.
- the graphite electrode 7 was consumed quickly, while when the connection of the terminals was reversed, the electrode 8 was consumed but not the electrode 7.
- the graphite electrode is consumed when I anode > I cathode , and it is not consumed when I anode ⁇ I ca t hoder where I anode is the current value in the periods in which the graphite electrode electrochemically acts as an anode electrode and I ca t hode is the current value in the periods in which the graphite electrode electrochemically acts as a cathode electrode.
- the inventors Based on this stabilization condition, the inventors have developed a novel electrolytic treatment method with which graphite electrodes can be maintained stable with an asymmetric waveform current.
- Fig. 3 is an explanatory diagram showing an example of a continuous electrolytic treatment method for metal webs according to the invention.
- the parts (3) through (6) of Fig. 2 show a variety of asymmetric waveforms which may be employed with the invention...
- a metal web 1 is passed through an auxiliary electrolytic cell 15 by a guide roll 16, and then through an electrolytic cell 4 via pass rolls 17 and 18 and a guide roll 2.
- the web 1 is conveyed horizontally by a backing roll 3.
- the web is moved out of the cell 4 by a roll 5.
- the auxiliary electrolytic cell has an auxiliary electrode, namely, an insoluble anode electrode 20 which is disposed confronting the metal web.
- the insoluble anode electrode is made of platinum or lead.
- a pump 10 is used to deliver the electrolytic solution 28 to an electrolytic solution supplying pipe 19 which debouches into the auxiliary electrolytic cell 15.
- the electrolytic solution thus delivered covers the insoluble anode electrode 20 and the metal web 1 in the cell 15, and is then returned to the tank 9 through a discharging pipe 21.
- the electrolytic cell 4 is divided by an insulator 6 into two parts in which respective graphite electrodes 7 and 8 are disposed confronting the metal web 1.
- the pump 10 supplies the electrolytic solution from the tank 9 to electrolytic solution supplying pipes 11 and 12 opening into the electrolytic cell 4.
- the electrolytic solution thus supplied is returned through the discharging pipe 13 to the tank 9.
- the electrolytic solution circulating system includes a heat exchanger and a filter so that the temperature of the electrolytic solution is controlled precisely and foreign matter is removed from the solution.
- a power source 14 is provided to apply an asymmetric alternate waveform current, for instance, having a waveform as shown in parts (3) through (6) of Fig. 2, to the electrolytic cell with the electrodes arranged as described.
- the positive terminal of the power source 14 is connected to the graphite electrode 7, and is further connected through a thyristor or diode 22 to the insoluble anode electrode 20 in the auxiliary electrolytic cell 16.
- the negative terminal of the power source is connected to the graphite electrode 8.
- the current In is applied to both the graphite electrode 7 and the insoluble anode electrode 20.
- the current thus applied which causes an anode reaction to occur on the surfaces of these electrodes, flows through the electrolytic solution to the metal web 1.
- a cathode reaction treatment occurs on the metal web 1 confronting the electrodes.
- the current In which flows in the metal web due to electron conduction, is returned through the electrolytic solution and the graphite electrode 8 to the power source 14.
- the. part of the metal web 1 which confronts the electrode 8 is subjected to an anode reaction treatment, while the surface of the electrode 8 is subjected to a cathode reaction treatment.
- control may be achieved, if a thyristor is employed, by controlling its ON time, or in the case of a diode, by inserting a variable resistor in its circuit.
- control may be achieved by adjusting the distance between the anode electrode 20 and the metal web 1, or by adjusting the effective area of the anode electrode 20.
- a separate electrolytic solution circulating tank (not shown) for the auxiliary electrolytic cell 15 can be provided so that the type of electrolytic solution and parameters thereof including its temperature and density can be varied.
- the current I r is supplied from the power source 14 to the graphite electrode 8, and is applied through the electrolytic solution to the metal web 1.
- an anode reaction treatment occurs on the surface of the graphite electrode 8
- a cathode reaction treatment occurs on the surface of the metal web 1.
- the current I r which flows in the metal web by electron conduction, is returned through the electrolytic solution and the graphite electrode 7 to the power source 14.
- a cathode reaction treatment occurs on the surface of the graphite electrode 7, while the part of the metal web 1 confronting the graphite electrode 7 is subjected to.an anode reaction treatment.
- the current I r does not flow to the anode electrode 20 due to the presence of the thyristor or diode.
- the electrodes 7 and 8 are considerably stable, being free from oxidation consumption.
- the current I anode therethrough is In
- the current I ca t hode therethrough is I r .
- In I r + ⁇
- In In + ⁇
- ⁇ > a are established, and therefore In ⁇ In.
- the stabilization condition is satisfied.
- the current I anode therethrough is I r
- the current .I ca t h od e therethrough is In. That is, since I r ⁇ In is established, the stabilization condition I anode ⁇ I ca t hode is maintained.
- the auxiliary electrode 20 in the auxiliary electrolytic cell 15 is always stable because it is an insoluble anode electrode, and only an anode reaction occurs therewith.
- the insoluble anode electrode 20 is positioned on one side of the metal web 1 opposite the side on which the graphite electrodes 7 and 8 are disposed.
- the electrodes are stable.
- an electrolytic reaction also occurs on the rear side of the metal web, thus forming a film thereon. This phenomenon is undesirable.
- the reaction efficiency is lowered as much.
- the system shown in Fig. 3 is usually preferable.
- a specific feature of the invention resides in that, in the electrolytic treatment system using an asymmetric waveform A.C. of the invention, a part of the current is applied to the auxiliary electrode so that the .graphite electrode stabilization condition I an od e ⁇ Icathode is established.
- Another specific feature of the invention resides in that the aforementioned condition is satisfied and the graphite electrodes and the insoluble anode electrode are arranged on the same side of the metal web so that the rear surface of the metal web is protected from unwanted reactions and, accordingly, so that the reaction efficiency is increased.
- the invention is not limited by the configuration of the electrolytic cell, the number of divisions of the electrolytic cell, the order of arrangement of the electrodes, or the type of the electrolytic cell.
- any asymmetric waveform A.C. may be used with the inventive electrolytic treatment method if it satisfies the asymmetric waveform condition In > I r .
- a continuous electrolytic grainning treatment was applied to art aluminum plate using the electrolytic treatment system shown in Fig. 3.
- the electrolytic solution employed was a 1% nitric acid solution at a temperature of 35°C, and an asymmetric waveform A.C. current as shown in part (5) of Fig. 2 was employed.
- the electrodes 7 and 8 were graphite electrodes, and the insoluble anode electrode 20 was made of platinum.
- the value ⁇ was varied by adjusting the effective electrolytic length of the insoluble anode electrode.
- the frequency was varied in a range of 30 Hz to 90 Hz.
- Table 1 the results obtained shown in Table 1 following were invariant under such frequency variations. That is, the currents I anode and I ca t hode and the consumption rate of the graphite electrodes 7 and 8 were as indicated in Table 1, independent of the frequency.
- the offset printing plate supports Nos. 3 and 4 in Table 1 had roughened surfaces which were excellent in quality.
- Example 2 Experiments were carried out under the same conditions as those of Example 1 except that the electrolytic solution was a 1% hydrochloric acid solution and the temperature was 35°C. The stability of the electrodes was the same as that in Table 1.
- a continuous anodic oxidation treatment was applied to aluminum plates using the electrolytic treatment system as shown in Fig. 3.
- the electrolytic solution was a 20% nitric acid solution at a temperature of 30°C, and an asymmetric waveform A.C... as indicated in part (4) of Fig. 4 was employed.
- the electrodes 7 and 8 were graphite electrodes, and the insoluble anode electrode 20 was made of lead.
- the forward current In was varied by adjusting the effective electrolytic length of the insoluble anode electrode. Also, the frequency was varied in the range of 30 Hz to 90 Hz. However, as above, the currents I anode and I cathode and the consumption rates of the graphite electrodes as indicated in Table 2 were found to be invariant with respect to frequency.
- the consumption rate of the electrodes is minimized with the use of the invention, with the result that a continuous electrolytic treatment of high efficiency and which is stable is obtained. Furthermore, secondary effects such as the elimination of the need for inspection and maintenance and a reduction in the manufacturing cost are provided.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electroplating Methods And Accessories (AREA)
- Electrochemical Coating By Surface Reaction (AREA)
- Electrolytic Production Of Metals (AREA)
- Printing Plates And Materials Therefor (AREA)
Abstract
Description
- The present invention relates to a method of electrolytic treatment on the surface of metal web with which the stability of graphite electrodes used in the electrolytic treatment of a metal plate is remarkably improved.
- Examples of a method of applying an electrolytic treatment to the surface of a metal member made of aluminum, iron or the like are the plating method, the electrolytic roughening method, the electrolytic etching method, the anodic oxidation method, the electrolytic coloring method, and the electrolytic satin finishing method, all which have been extensively employed in the art. D.C. sources, power mains A.C. sources, superposed-waveform current sources, and thyristor-controlled special-waveform or square-wave A.C. sources have been employed with these methods in order to meet requirements of quality of the electrolytic treatment or to improve the reaction efficiency. For instance, GB 1,548,689 discloses a process in which an A.C. is applied in the electrolytic treatment of an aluminum plate with the voltage applied to the anode electrode being higher than that applied to the cathode electrode, whereby an aluminum
- substrate for lithographic printing whose surface is electrograined satisfactorily is obtained. When using a regulated A.C.,
- it is essential to employ electrodes which are highly stable. In general, platinum, tantalum, titanium, iron, lead and graphite are employed as electrode materials. Graphite electrodes are widely employed because they are chemically relatively stable and are of low cost. Fig. 1 shows an example of a conventional continuous electrolytic treatment system for metal webs which utilizes graphite electrodes. In this system, a
metal web 1 is introduced into anelectrolytic cell 4. while being guided by aguide roll 2, and is conveyed horizontally through the cell while being supported by aroll 3. Finally, theweb 1 is moved out of the cell passing around aguide roll 5. Theelectrolytic cell 4 is divided by aninsulator 6 into two chambers in which graphite electrodes are arranged on both sides of themetal web 1. A supply ofelectrolytic solution 28 is stored in atank 9. Apump 10 supplies theelectrolytic solution 28 to electrolyticsolution supplying pipes electrolytic cell 4. The electrolytic solution thus supplied covers thegraphite electrodes tank 9 through adischarging pipe 13. Apower source 14 connected to thegraphite electrodes metal web 1 with this system. - The
power source 14, may produce (1) direct current, (2) symmetric alternate current waveform, (3) and (4) asymmetric alternate current waveform, and (5) and (6) asymmetric square-wave alternate current waveform as shown in Fig. 2. In general, in such an A.C. waveform, the average value of the forward current In is not equal to the average value of the reverse current Ir. - A graphite electrode is considerably stable when used as a cathode electrode. However, when a graphite electrode is used as an anode electrode, it is consumed in the electrolytic solution, forming C02 by anode oxidation and, at the same time, it decays due to erosion of the graphite interlayers, which occurs at a rate depending on electrolytic conditions. When decay occurs, the current distribution in the electrode changes so that the electrolytic treatment becomes nonuniform. Therefore, the occurrence of such a phenomenon should be avoided in a case where the electrolytic treatment must be done with high accuracy. Accordingly, it is necessary to replace the electrodes periodically. This requirement is a drawback for mass production, and is one of the factors which lowers productivity.
- The inventors have conducted intensive research regarding ways to prevent the consumption of graphite electrodes, and found conditions exist under which graphite electrodes employed in a system using asymmetric waveform A.C. can be stabilized. Specifically, in the electrolytic cell shown in Fig. 1, an asymmetric waveform current (In > Ir) as shown at (4) in Fig. 2 was used. The forward terminal was connected to the
electrode 7 and the reverse terminal to theelectrode 8. Under these conditions, an electrolytic treatment was carried out by using a 1% HC1 electrolytic bath with a current density of 50 A/dm2 and a frequency of 60 Hz. In this case, thegraphite electrode 7 was consumed quickly, while when the connection of the terminals was reversed, theelectrode 8 was consumed but not theelectrode 7. This means that, for the use of an asymmetric waveform current, the graphite electrode is consumed when Ianode > Icathode, and it is not consumed when Ianode < Icathoder where Ianode is the current value in the periods in which the graphite electrode electrochemically acts as an anode electrode and Icathode is the current value in the periods in which the graphite electrode electrochemically acts as a cathode electrode. - Based on this stabilization condition, the inventors have developed a novel electrolytic treatment method with which graphite electrodes can be maintained stable with an asymmetric waveform current.
-
- Fig. 1 is an explanatory diagram schematically showing an example of a conventional continuous electrolytic treatment system;"
- Fig. 2 is a diagram showing current waveforms for a description of the invention; and
- Figs. 3, 4 and 5 are explanatory diagrams schematically showing examples of continuous electrolytic treatment systems for practicing an electrolytic treatment method according to the invention.
- The invention will now be described in detail with reference to preferred embodiments shown in Figs. 3, 4 and 5.
- Fig. 3 is an explanatory diagram showing an example of a continuous electrolytic treatment method for metal webs according to the invention. The parts (3) through (6) of Fig. 2 show a variety of asymmetric waveforms which may be employed with the invention...
- First, a
metal web 1 is passed through an auxiliaryelectrolytic cell 15 by aguide roll 16, and then through anelectrolytic cell 4 viapass rolls 17 and 18 and aguide roll 2. In theelectrolytic cell 4, theweb 1 is conveyed horizontally by abacking roll 3. Finally, the web is moved out of thecell 4 by aroll 5. - The auxiliary electrolytic cell has an auxiliary electrode, namely, an
insoluble anode electrode 20 which is disposed confronting the metal web. The insoluble anode electrode is made of platinum or lead. Apump 10 is used to deliver theelectrolytic solution 28 to an electrolyticsolution supplying pipe 19 which debouches into the auxiliaryelectrolytic cell 15. The electrolytic solution thus delivered covers theinsoluble anode electrode 20 and themetal web 1 in thecell 15, and is then returned to thetank 9 through adischarging pipe 21. - The
electrolytic cell 4 is divided by aninsulator 6 into two parts in whichrespective graphite electrodes metal web 1. Thepump 10 supplies the electrolytic solution from thetank 9 to electrolyticsolution supplying pipes electrolytic cell 4. The electrolytic solution thus supplied is returned through thedischarging pipe 13 to thetank 9. In general, the electrolytic solution circulating system includes a heat exchanger and a filter so that the temperature of the electrolytic solution is controlled precisely and foreign matter is removed from the solution. - A
power source 14 is provided to apply an asymmetric alternate waveform current, for instance, having a waveform as shown in parts (3) through (6) of Fig. 2, to the electrolytic cell with the electrodes arranged as described. The current waveform is such that In > Ir and In = Ir + a are maintained, where In is the forward current value and Ir is the reverse current value. The positive terminal of thepower source 14 is connected to thegraphite electrode 7, and is further connected through a thyristor ordiode 22 to theinsoluble anode electrode 20 in the auxiliaryelectrolytic cell 16. The negative terminal of the power source is connected to thegraphite electrode 8. - In the forward period (positive half cycle) of the current flow, the current In is applied to both the
graphite electrode 7 and theinsoluble anode electrode 20. The current thus applied, which causes an anode reaction to occur on the surfaces of these electrodes, flows through the electrolytic solution to themetal web 1. At the same time, a cathode reaction treatment occurs on themetal web 1 confronting the electrodes. The current In, which flows in the metal web due to electron conduction, is returned through the electrolytic solution and thegraphite electrode 8 to thepower source 14. In this operation, the. part of themetal web 1 which confronts theelectrode 8 is subjected to an anode reaction treatment, while the surface of theelectrode 8 is subjected to a cathode reaction treatment. - Assuming that the currents applied to the
graphite electrode 7 and theinsoluble anode electrode 20 are represented by In' and β, respectively, then control is carried out so as to satisfy the following condition: - β > α.
- Such control may be achieved, if a thyristor is employed, by controlling its ON time, or in the case of a diode, by inserting a variable resistor in its circuit. Alternatively, control may be achieved by adjusting the distance between the
anode electrode 20 and themetal web 1, or by adjusting the effective area of theanode electrode 20. Further, a separate electrolytic solution circulating tank (not shown) for the auxiliaryelectrolytic cell 15 can be provided so that the type of electrolytic solution and parameters thereof including its temperature and density can be varied. - In the reverse current period (negative half cycle), the current Ir is supplied from the
power source 14 to thegraphite electrode 8, and is applied through the electrolytic solution to themetal web 1. In this operation, an anode reaction treatment occurs on the surface of thegraphite electrode 8, while a cathode reaction treatment occurs on the surface of themetal web 1. The current Ir, which flows in the metal web by electron conduction, is returned through the electrolytic solution and thegraphite electrode 7 to thepower source 14. In this operation, a cathode reaction treatment occurs on the surface of thegraphite electrode 7, while the part of themetal web 1 confronting thegraphite electrode 7 is subjected to.an anode reaction treatment. In the reverse period, the current Ir does not flow to theanode electrode 20 due to the presence of the thyristor or diode. - In the above-described electrolytic treatment method according to the invention, the
electrodes graphite electrode 7 acts as an anode electrode, the current Ianode therethrough is In, and when it acts as a cathode electrode, the current Icathode therethrough is Ir. In this case, In = Ir + α, In = In + β, and β > a are established, and therefore In < In. Accordingly, for thegraphite electrode 7, Ianode < Icathode. Thus, the stabilization condition is satisfied. On the other hand, when thegraphite electrode 8 acts as an anode electrode, the current Ianode therethrough is Ir, and when it acts as a cathode electrode, the current .Icathode therethrough is In. That is, since Ir < In is established, the stabilization condition Ianode < Icathode is maintained. Theauxiliary electrode 20 in the auxiliaryelectrolytic cell 15 is always stable because it is an insoluble anode electrode, and only an anode reaction occurs therewith. - In electrolytic treatment system shown in Figs. 4 and 5, in which figures those components which have been described with reference to Fig. 3 are designated by the same reference numerals, the
insoluble anode electrode 20 is positioned on one side of themetal web 1 opposite the side on which thegraphite electrodes - As is apparent from the above description, a specific feature of the invention resides in that, in the electrolytic treatment system using an asymmetric waveform A.C. of the invention, a part of the current is applied to the auxiliary electrode so that the .graphite electrode stabilization condition Ianode < Icathode is established. Another specific feature of the invention resides in that the aforementioned condition is satisfied and the graphite electrodes and the insoluble anode electrode are arranged on the same side of the metal web so that the rear surface of the metal web is protected from unwanted reactions and, accordingly, so that the reaction efficiency is increased. The invention is not limited by the configuration of the electrolytic cell, the number of divisions of the electrolytic cell, the order of arrangement of the electrodes, or the type of the electrolytic cell. In addition, any asymmetric waveform A.C. may be used with the inventive electrolytic treatment method if it satisfies the asymmetric waveform condition In > Ir.
- In order to clarify the effects of the invention, specific examples of the electrolytic treatment method according to the invention will be described.
- In order to prepare an offset printing plate support, a continuous electrolytic grainning treatment was applied to art aluminum plate using the electrolytic treatment system shown in Fig. 3. The electrolytic solution employed was a 1% nitric acid solution at a temperature of 35°C, and an asymmetric waveform A.C. current as shown in part (5) of Fig. 2 was employed. The
electrodes insoluble anode electrode 20 was made of platinum. After the electrolytic treatment was carried out with a forward current of In = 300 A and a reverse current of Ir = 270 A at a treatment rate of 1 m/min for twenty hours, the surfaces of the graphite electrodes were visually inspected for consumption and decay. - In addition, in order to apply a part of the forward current In to the insoluble anode electrode, the value β was varied by adjusting the effective electrolytic length of the insoluble anode electrode. Also, the frequency was varied in a range of 30 Hz to 90 Hz. However, the results obtained shown in Table 1 following were invariant under such frequency variations. That is, the currents Ianode and Icathode and the consumption rate of the
graphite electrodes - The offset printing plate supports Nos. 3 and 4 in Table 1 had roughened surfaces which were excellent in quality.
-
- Legend
- ○: The electrode was not consumed at all.
- Δ: The electrode was slightly consumed.
- X : The electrode was consumed greatly and the surface decayed.
- In order to fabricate offset printing plate supports, a continuous anodic oxidation treatment was applied to aluminum plates using the electrolytic treatment system as shown in Fig. 3. The electrolytic solution was a 20% nitric acid solution at a temperature of 30°C, and an asymmetric waveform A.C... as indicated in part (4) of Fig. 4 was employed. The
electrodes insoluble anode electrode 20 was made of lead. After the electrolytic treatment was carried out with a forward current of In = 60 A and a reverse current of Ir = 50 A at a treatment rate of I m/min for twenty hours, the surfaces of the graphite electrodes were visually inspected for consumption and decay. In order to apply a part of the forward current In to the insoluble anode electrode, the forward current In was varied by adjusting the effective electrolytic length of the insoluble anode electrode. Also, the frequency was varied in the range of 30 Hz to 90 Hz. However, as above, the currents Ianode and Icathode and the consumption rates of the graphite electrodes as indicated in Table 2 were found to be invariant with respect to frequency. -
- 0 : The electrode was not consumed at all.
- Δ: The electrode was slightly consumed.
- ×: The electrode was consumed greatly and the surface decayed.
- As is apparent from the above description, the consumption rate of the electrodes is minimized with the use of the invention, with the result that a continuous electrolytic treatment of high efficiency and which is stable is obtained. Furthermore, secondary effects such as the elimination of the need for inspection and maintenance and a reduction in the manufacturing cost are provided.
- While the invention has been described with reference to preferred embodiments, it should be noted that the invention has a wide range of applications.
Claims (7)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP86619/83 | 1983-05-19 | ||
JP58086619A JPS59215500A (en) | 1983-05-19 | 1983-05-19 | Electrolytic treatment |
Publications (3)
Publication Number | Publication Date |
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EP0129338A2 true EP0129338A2 (en) | 1984-12-27 |
EP0129338A3 EP0129338A3 (en) | 1986-11-20 |
EP0129338B1 EP0129338B1 (en) | 1989-09-20 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP84303393A Expired EP0129338B1 (en) | 1983-05-19 | 1984-05-18 | Electrolytic treatment method |
Country Status (5)
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US (1) | US4533444A (en) |
EP (1) | EP0129338B1 (en) |
JP (1) | JPS59215500A (en) |
CA (1) | CA1235383A (en) |
DE (1) | DE3479824D1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0349983A2 (en) * | 1988-07-04 | 1990-01-10 | Fuji Photo Film Co., Ltd. | Electrolytic treatment apparatus |
EP0387750A1 (en) * | 1989-03-14 | 1990-09-19 | Fuji Photo Film Co., Ltd. | Electrolytic treatment apparatus |
EP0445959A1 (en) * | 1990-03-06 | 1991-09-11 | Du Pont (UK) Limited | Electrolytic graining |
EP0730979A3 (en) * | 1995-03-06 | 1997-08-20 | Fuji Photo Film Co Ltd | Support for lithographic printing plate, process for the preparation thereof and electrochemical roughening apparatus |
EP0812705A1 (en) * | 1996-06-12 | 1997-12-17 | Konica Corporation | Method of manufacturing support for planographic printing plate |
US7685712B2 (en) | 2005-01-27 | 2010-03-30 | Snecma | Method for repairing a rubbing surface of a turbomachine variable-pitch blade |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0620029B2 (en) * | 1984-08-30 | 1994-03-16 | 松下電器産業株式会社 | Etching method for electrode foil for aluminum electrolytic capacitors |
JPH0616469B2 (en) * | 1984-12-28 | 1994-03-02 | 松下電器産業株式会社 | Etching method for electrode foil for aluminum electrolytic capacitors |
JPH0637716B2 (en) * | 1987-08-21 | 1994-05-18 | 富士写真フイルム株式会社 | Electrolytic treatment method |
JPH0191227U (en) * | 1987-12-10 | 1989-06-15 | ||
US5271818A (en) * | 1989-03-30 | 1993-12-21 | Hoechst Aktiengesellschaft | Apparatus for roughening a substrate for photosensitive layers |
US5164033A (en) * | 1990-04-17 | 1992-11-17 | Tir Systems Ltd. | Electro-chemical etch device |
JPH041413U (en) * | 1990-04-20 | 1992-01-08 | ||
JPH0939431A (en) * | 1995-07-31 | 1997-02-10 | Fuji Photo Film Co Ltd | Method of roughening support body for lithographic printing plate |
DE19545231A1 (en) * | 1995-11-21 | 1997-05-22 | Atotech Deutschland Gmbh | Process for the electrolytic deposition of metal layers |
ZA200906786B (en) * | 2008-10-16 | 2010-05-26 | Internat Advanced Res Ct Arci | A process for continuous coating deposition and an apparatus for carrying out the process |
JP5178502B2 (en) * | 2008-12-26 | 2013-04-10 | 富士フイルム株式会社 | Feed connection structure and electrolytic treatment apparatus |
WO2011072025A2 (en) * | 2009-12-08 | 2011-06-16 | Bill Culwell | Water closet flange seal |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2901412A (en) * | 1955-12-09 | 1959-08-25 | Reynolds Metals Co | Apparatus for anodizing aluminum surfaces |
US2951025A (en) * | 1957-06-13 | 1960-08-30 | Reynolds Metals Co | Apparatus for anodizing aluminum |
GB2053272A (en) * | 1979-05-30 | 1981-02-04 | Fuji Photo Film Co Ltd | Electrolytic graining a support for a lithographic printing plate |
DE3030815A1 (en) * | 1979-08-15 | 1981-03-26 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | ELECTROLYTIC GRIT PROCESS |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1548689A (en) * | 1975-11-06 | 1979-07-18 | Nippon Light Metal Res Labor | Process for electrograining aluminum substrates for lithographic printing |
US4214961A (en) * | 1979-03-01 | 1980-07-29 | Swiss Aluminium Ltd. | Method and apparatus for continuous electrochemical treatment of a metal web |
US4297184A (en) * | 1980-02-19 | 1981-10-27 | United Chemi-Con, Inc. | Method of etching aluminum |
US4315806A (en) * | 1980-09-19 | 1982-02-16 | Sprague Electric Company | Intermittent AC etching of aluminum foil |
-
1983
- 1983-05-19 JP JP58086619A patent/JPS59215500A/en active Granted
-
1984
- 1984-05-17 US US06/611,288 patent/US4533444A/en not_active Expired - Lifetime
- 1984-05-18 EP EP84303393A patent/EP0129338B1/en not_active Expired
- 1984-05-18 CA CA000454744A patent/CA1235383A/en not_active Expired
- 1984-05-18 DE DE8484303393T patent/DE3479824D1/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2901412A (en) * | 1955-12-09 | 1959-08-25 | Reynolds Metals Co | Apparatus for anodizing aluminum surfaces |
US2951025A (en) * | 1957-06-13 | 1960-08-30 | Reynolds Metals Co | Apparatus for anodizing aluminum |
GB2053272A (en) * | 1979-05-30 | 1981-02-04 | Fuji Photo Film Co Ltd | Electrolytic graining a support for a lithographic printing plate |
DE3030815A1 (en) * | 1979-08-15 | 1981-03-26 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | ELECTROLYTIC GRIT PROCESS |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0349983A2 (en) * | 1988-07-04 | 1990-01-10 | Fuji Photo Film Co., Ltd. | Electrolytic treatment apparatus |
EP0349983A3 (en) * | 1988-07-04 | 1990-09-19 | Fuji Photo Film Co., Ltd. | Electrolytic treatment apparatus |
EP0387750A1 (en) * | 1989-03-14 | 1990-09-19 | Fuji Photo Film Co., Ltd. | Electrolytic treatment apparatus |
US5094733A (en) * | 1989-03-14 | 1992-03-10 | Fuji Photo Co., Ltd. | Electrolytic treatment apparatus |
EP0445959A1 (en) * | 1990-03-06 | 1991-09-11 | Du Pont (UK) Limited | Electrolytic graining |
EP0730979A3 (en) * | 1995-03-06 | 1997-08-20 | Fuji Photo Film Co Ltd | Support for lithographic printing plate, process for the preparation thereof and electrochemical roughening apparatus |
US5837345A (en) * | 1995-03-06 | 1998-11-17 | Fuji Photo Film Co., Ltd. | Support for lithographic printing plate, process for the preparation thereof and electrochemical roughening apparatus |
EP0812705A1 (en) * | 1996-06-12 | 1997-12-17 | Konica Corporation | Method of manufacturing support for planographic printing plate |
US6015649A (en) * | 1996-06-12 | 2000-01-18 | Konica Corporation | Method of manufacturing support for planographic printing plate |
US7685712B2 (en) | 2005-01-27 | 2010-03-30 | Snecma | Method for repairing a rubbing surface of a turbomachine variable-pitch blade |
Also Published As
Publication number | Publication date |
---|---|
JPS59215500A (en) | 1984-12-05 |
DE3479824D1 (en) | 1989-10-26 |
CA1235383A (en) | 1988-04-19 |
US4533444A (en) | 1985-08-06 |
EP0129338A3 (en) | 1986-11-20 |
EP0129338B1 (en) | 1989-09-20 |
JPS6237718B2 (en) | 1987-08-13 |
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